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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2017-03-16 03:42:36 UTC

Update Date

2022-03-07 03:17:52 UTC

HMDB ID

HMDB0062310

Secondary Accession Numbers

HMDB62310

Metabolite Identification

Common Name

1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate

Description

1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate is classified as a member of the 1-acylglycerol-3-phosphates. 1-acylglycerol-3-phosphates are lysophosphatidic acids where the glycerol is esterified with a fatty acid at O-1 position. 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate is considered to be practically insoluble (in water) and acidic. 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate is a glycerophosphate lipid molecule

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

  Mrv1652303161704422D          

 42 41  0  0  1  0            999 V2000
    2.8066    6.5704    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    5.7454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    5.7454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    5.7454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921    5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    5.7454    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921    4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6632    4.5079    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6632    2.8579    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    1.6204    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    0.7954    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    0.7954    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    1.6204    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224    4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2368    2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658    2.8579    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9513    2.4454    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3802    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0947    2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092    3.2704    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   13.5237    3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2217    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3967    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  6  0  0  0
 34 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 39 42  2  0  0  0  0
M  END

HMDB0062310
     RDKit          3D
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate
 76 75  0  0  0  0  0  0  0  0999 V2000
   11.9628    1.3544    1.0304 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0618    2.4876    0.6647 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8510    2.0356   -0.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0170    1.0504    0.6300 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8349    0.6646   -0.2747 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9981    1.7996   -0.6463 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7361    1.9828   -0.3759 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8228    1.1332    0.3582 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2345   -0.1023    0.9507 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8351   -1.2894    0.6854 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8702   -1.8005   -0.2695 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1788   -0.9369   -1.1907 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8936   -0.7555   -1.2334 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8794   -1.3953   -0.3461 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1805   -0.2943    0.3394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1009   -0.0757    0.2371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9761   -0.9176   -0.5825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0349   -1.5441    0.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9330   -2.4231   -0.4829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6184   -1.6259   -1.5557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4494   -0.5396   -0.9270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4703   -1.1672   -0.0512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1913   -1.4211    1.1371 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7128   -1.4692   -0.5346 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7829   -2.0429    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3137   -1.1895    1.2435 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.3968   -0.9336    2.2274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7343    0.1564    0.6410 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2841    0.8882    1.6932 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7914    2.4178    1.1334 P   0  0  0  0  0  5  0  0  0  0  0  0
  -10.9758    3.3687    2.2929 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2694    2.1553    0.3296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6852    3.0772    0.0556 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0041    1.5428    0.6359 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0059    1.2737    2.1513 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6673    0.3789    0.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6865    3.0652    1.5141 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6139    3.2022    0.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2360    1.6063   -1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2782    2.9439   -0.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6478    0.1561    0.8123 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6797    1.4120    1.5983 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4163    0.4137   -1.2556 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3901   -0.2831   -0.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4675    2.6300   -1.2401 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2790    2.9300   -0.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8771    1.0251   -0.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4176    1.8442    1.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0019    0.0039    1.7750 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3332   -2.0966    1.3204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1132   -2.4389    0.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3828   -2.6630   -0.8891 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7862   -0.3982   -1.9505 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4913   -0.0614   -1.9959 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3218   -2.0251    0.4604 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2735   -2.0638   -0.9540 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7714    0.3700    0.9641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5356    0.7864    0.7979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5380   -0.2021   -1.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5286   -1.6525   -1.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5054   -2.2346    1.0635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5502   -0.7774    0.9179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2754   -3.2021   -0.9416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6720   -2.8911    0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8938   -1.2362   -2.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3251   -2.3532   -2.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9353    0.1063   -1.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7678    0.1485   -0.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6046   -2.2422   -0.6210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4758   -3.0416    0.5677 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2352   -1.6567    1.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4616   -1.5611    2.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4606   -0.0199   -0.1789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8034    0.6166    0.2549 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2095    2.4456   -0.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0003    3.5516    0.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  2  0
 30 32  1  0
 30 33  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  0
  2 38  1  0
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  5 43  1  0
  5 44  1  0
  6 45  1  0
  7 46  1  0
  8 47  1  0
  8 48  1  0
  9 49  1  0
 10 50  1  0
 11 51  1  0
 11 52  1  0
 12 53  1  0
 13 54  1  0
 14 55  1  0
 14 56  1  0
 15 57  1  0
 16 58  1  0
 17 59  1  0
 17 60  1  0
 18 61  1  0
 18 62  1  0
 19 63  1  0
 19 64  1  0
 20 65  1  0
 20 66  1  0
 21 67  1  0
 21 68  1  0
 25 69  1  0
 25 70  1  0
 26 71  1  1
 27 72  1  0
 28 73  1  0
 28 74  1  0
 32 75  1  0
 33 76  1  0
M  END

  Mrv1652303161704422D          

 42 41  0  0  1  0            999 V2000
    2.8066    6.5704    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    5.7454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    5.7454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    5.7454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921    5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    5.7454    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921    4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6632    4.5079    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6632    2.8579    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    1.6204    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    0.7954    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    0.7954    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    1.6204    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224    4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2368    2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658    2.8579    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9513    2.4454    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3802    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0947    2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092    3.2704    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   13.5237    3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2217    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3967    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  6  0  0  0
 34 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 39 42  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0062310

> <DATABASE_NAME>
hmdb

> <SMILES>
[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCCCC(=O)OC[C@@]([H])(O)COP(O)(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H43O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25(27)31-22-24(26)23-32-33(28,29)30/h6-7,9-10,12-13,15-16,24,26H,2-5,8,11,14,17-23H2,1H3,(H2,28,29,30)/b7-6-,10-9-,13-12-,16-15-/t24-/m1/s1

> <INCHI_KEY>
KSDVXYAHZXLGDS-XSQXPFHXSA-N

> <FORMULA>
C25H43O7P

> <MOLECULAR_WEIGHT>
486.586

> <EXACT_MASS>
486.274640723

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
55.31020002132722

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R)-3-[(7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoyloxy]-2-hydroxypropoxy]phosphonic acid

> <ALOGPS_LOGP>
5.67

> <JCHEM_LOGP>
6.1781992116666675

> <ALOGPS_LOGS>
-5.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.531115837556447

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.505317785248875

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4039997949880583

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
137.05280000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
22

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.43e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-3-[(7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoyloxy]-2-hydroxypropoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0062310
     RDKit          3D
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate
 76 75  0  0  0  0  0  0  0  0999 V2000
   11.9628    1.3544    1.0304 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0618    2.4876    0.6647 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8510    2.0356   -0.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0170    1.0504    0.6300 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8349    0.6646   -0.2747 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9981    1.7996   -0.6463 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7361    1.9828   -0.3759 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8228    1.1332    0.3582 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2345   -0.1023    0.9507 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8351   -1.2894    0.6854 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8702   -1.8005   -0.2695 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1788   -0.9369   -1.1907 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8936   -0.7555   -1.2334 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8794   -1.3953   -0.3461 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1805   -0.2943    0.3394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1009   -0.0757    0.2371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9761   -0.9176   -0.5825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0349   -1.5441    0.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9330   -2.4231   -0.4829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6184   -1.6259   -1.5557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4494   -0.5396   -0.9270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4703   -1.1672   -0.0512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1913   -1.4211    1.1371 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7128   -1.4692   -0.5346 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7829   -2.0429    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3137   -1.1895    1.2435 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.3968   -0.9336    2.2274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7343    0.1564    0.6410 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2841    0.8882    1.6932 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7914    2.4178    1.1334 P   0  0  0  0  0  5  0  0  0  0  0  0
  -10.9758    3.3687    2.2929 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2694    2.1553    0.3296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6852    3.0772    0.0556 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0041    1.5428    0.6359 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0059    1.2737    2.1513 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6673    0.3789    0.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6865    3.0652    1.5141 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6139    3.2022    0.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2360    1.6063   -1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2782    2.9439   -0.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6478    0.1561    0.8123 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6797    1.4120    1.5983 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4163    0.4137   -1.2556 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3901   -0.2831   -0.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4675    2.6300   -1.2401 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2790    2.9300   -0.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8771    1.0251   -0.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4176    1.8442    1.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0019    0.0039    1.7750 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3332   -2.0966    1.3204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1132   -2.4389    0.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3828   -2.6630   -0.8891 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7862   -0.3982   -1.9505 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4913   -0.0614   -1.9959 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3218   -2.0251    0.4604 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2735   -2.0638   -0.9540 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7714    0.3700    0.9641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5356    0.7864    0.7979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5380   -0.2021   -1.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5286   -1.6525   -1.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5054   -2.2346    1.0635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5502   -0.7774    0.9179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2754   -3.2021   -0.9416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6720   -2.8911    0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8938   -1.2362   -2.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3251   -2.3532   -2.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9353    0.1063   -1.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7678    0.1485   -0.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6046   -2.2422   -0.6210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4758   -3.0416    0.5677 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2352   -1.6567    1.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4616   -1.5611    2.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4606   -0.0199   -0.1789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8034    0.6166    0.2549 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2095    2.4456   -0.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0003    3.5516    0.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  2  0
 30 32  1  0
 30 33  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  0
  2 38  1  0
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  5 43  1  0
  5 44  1  0
  6 45  1  0
  7 46  1  0
  8 47  1  0
  8 48  1  0
  9 49  1  0
 10 50  1  0
 11 51  1  0
 11 52  1  0
 12 53  1  0
 13 54  1  0
 14 55  1  0
 14 56  1  0
 15 57  1  0
 16 58  1  0
 17 59  1  0
 17 60  1  0
 18 61  1  0
 18 62  1  0
 19 63  1  0
 19 64  1  0
 20 65  1  0
 20 66  1  0
 21 67  1  0
 21 68  1  0
 25 69  1  0
 25 70  1  0
 26 71  1  1
 27 72  1  0
 28 73  1  0
 28 74  1  0
 32 75  1  0
 33 76  1  0
M  END

HEADER    PROTEIN                                 16-MAR-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-MAR-17         0                                  
HETATM    1  H   UNK     0       5.239  12.265   0.000  0.00  0.00           H+0
HETATM    2  C   UNK     0       5.239  10.725   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.573   9.955   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.906  10.725   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.240   9.955   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.574  10.725   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.907   9.955   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.905   9.955   0.000  0.00  0.00           C+0
HETATM    9  H   UNK     0       2.572  10.725   0.000  0.00  0.00           H+0
HETATM   10  C   UNK     0       3.905   8.415   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.572   7.645   0.000  0.00  0.00           C+0
HETATM   12  H   UNK     0       1.238   8.415   0.000  0.00  0.00           H+0
HETATM   13  C   UNK     0       2.572   6.105   0.000  0.00  0.00           C+0
HETATM   14  H   UNK     0       1.238   5.335   0.000  0.00  0.00           H+0
HETATM   15  C   UNK     0       3.905   5.335   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.905   3.795   0.000  0.00  0.00           C+0
HETATM   17  H   UNK     0       2.572   3.025   0.000  0.00  0.00           H+0
HETATM   18  C   UNK     0       5.239   3.025   0.000  0.00  0.00           C+0
HETATM   19  H   UNK     0       5.239   1.485   0.000  0.00  0.00           H+0
HETATM   20  C   UNK     0       6.573   3.795   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.906   3.025   0.000  0.00  0.00           C+0
HETATM   22  H   UNK     0       7.906   1.485   0.000  0.00  0.00           H+0
HETATM   23  C   UNK     0       9.240   3.795   0.000  0.00  0.00           C+0
HETATM   24  H   UNK     0      10.574   3.025   0.000  0.00  0.00           H+0
HETATM   25  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.574   6.105   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.907   5.335   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.241   6.105   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.575   5.335   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      15.908   6.105   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      15.908   7.645   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      17.242   5.335   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      18.576   6.105   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      19.909   5.335   0.000  0.00  0.00           C+0
HETATM   35  H   UNK     0      18.576   4.565   0.000  0.00  0.00           H+0
HETATM   36  O   UNK     0      19.909   3.795   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      21.243   6.105   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      22.577   5.335   0.000  0.00  0.00           O+0
HETATM   39  P   UNK     0      23.910   6.105   0.000  0.00  0.00           P+0
HETATM   40  O   UNK     0      25.244   6.875   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      24.680   4.771   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      23.140   7.438   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    2    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   34   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41   42                                             
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   39                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   82    0
END

COMPND    HMDB0062310
HETATM    1  C1  UNL     1      11.963   1.354   1.030  1.00  0.00           C  
HETATM    2  C2  UNL     1      11.062   2.488   0.665  1.00  0.00           C  
HETATM    3  C3  UNL     1       9.851   2.036  -0.137  1.00  0.00           C  
HETATM    4  C4  UNL     1       9.017   1.050   0.630  1.00  0.00           C  
HETATM    5  C5  UNL     1       7.835   0.665  -0.275  1.00  0.00           C  
HETATM    6  C6  UNL     1       6.998   1.800  -0.646  1.00  0.00           C  
HETATM    7  C7  UNL     1       5.736   1.983  -0.376  1.00  0.00           C  
HETATM    8  C8  UNL     1       4.823   1.133   0.358  1.00  0.00           C  
HETATM    9  C9  UNL     1       5.234  -0.102   0.951  1.00  0.00           C  
HETATM   10  C10 UNL     1       4.835  -1.289   0.685  1.00  0.00           C  
HETATM   11  C11 UNL     1       3.870  -1.801  -0.269  1.00  0.00           C  
HETATM   12  C12 UNL     1       3.179  -0.937  -1.191  1.00  0.00           C  
HETATM   13  C13 UNL     1       1.894  -0.756  -1.233  1.00  0.00           C  
HETATM   14  C14 UNL     1       0.879  -1.395  -0.346  1.00  0.00           C  
HETATM   15  C15 UNL     1       0.180  -0.294   0.339  1.00  0.00           C  
HETATM   16  C16 UNL     1      -1.101  -0.076   0.237  1.00  0.00           C  
HETATM   17  C17 UNL     1      -1.976  -0.918  -0.583  1.00  0.00           C  
HETATM   18  C18 UNL     1      -3.035  -1.544   0.339  1.00  0.00           C  
HETATM   19  C19 UNL     1      -3.933  -2.423  -0.483  1.00  0.00           C  
HETATM   20  C20 UNL     1      -4.618  -1.626  -1.556  1.00  0.00           C  
HETATM   21  C21 UNL     1      -5.449  -0.540  -0.927  1.00  0.00           C  
HETATM   22  C22 UNL     1      -6.470  -1.167  -0.051  1.00  0.00           C  
HETATM   23  O1  UNL     1      -6.191  -1.421   1.137  1.00  0.00           O  
HETATM   24  O2  UNL     1      -7.713  -1.469  -0.535  1.00  0.00           O  
HETATM   25  C23 UNL     1      -8.783  -2.043   0.133  1.00  0.00           C  
HETATM   26  C24 UNL     1      -9.314  -1.189   1.243  1.00  0.00           C  
HETATM   27  O3  UNL     1      -8.397  -0.934   2.227  1.00  0.00           O  
HETATM   28  C25 UNL     1      -9.734   0.156   0.641  1.00  0.00           C  
HETATM   29  O4  UNL     1     -10.284   0.888   1.693  1.00  0.00           O  
HETATM   30  P1  UNL     1     -10.791   2.418   1.133  1.00  0.00           P  
HETATM   31  O5  UNL     1     -10.976   3.369   2.293  1.00  0.00           O  
HETATM   32  O6  UNL     1     -12.269   2.155   0.330  1.00  0.00           O  
HETATM   33  O7  UNL     1      -9.685   3.077   0.056  1.00  0.00           O  
HETATM   34  H1  UNL     1      13.004   1.543   0.636  1.00  0.00           H  
HETATM   35  H2  UNL     1      12.006   1.274   2.151  1.00  0.00           H  
HETATM   36  H3  UNL     1      11.667   0.379   0.626  1.00  0.00           H  
HETATM   37  H4  UNL     1      10.687   3.065   1.514  1.00  0.00           H  
HETATM   38  H5  UNL     1      11.614   3.202   0.005  1.00  0.00           H  
HETATM   39  H6  UNL     1      10.236   1.606  -1.083  1.00  0.00           H  
HETATM   40  H7  UNL     1       9.278   2.944  -0.401  1.00  0.00           H  
HETATM   41  H8  UNL     1       9.648   0.156   0.812  1.00  0.00           H  
HETATM   42  H9  UNL     1       8.680   1.412   1.598  1.00  0.00           H  
HETATM   43  H10 UNL     1       8.416   0.414  -1.256  1.00  0.00           H  
HETATM   44  H11 UNL     1       7.390  -0.283  -0.049  1.00  0.00           H  
HETATM   45  H12 UNL     1       7.467   2.630  -1.240  1.00  0.00           H  
HETATM   46  H13 UNL     1       5.279   2.930  -0.761  1.00  0.00           H  
HETATM   47  H14 UNL     1       3.877   1.025  -0.194  1.00  0.00           H  
HETATM   48  H15 UNL     1       4.418   1.844   1.230  1.00  0.00           H  
HETATM   49  H16 UNL     1       6.002   0.004   1.775  1.00  0.00           H  
HETATM   50  H17 UNL     1       5.333  -2.097   1.320  1.00  0.00           H  
HETATM   51  H18 UNL     1       3.113  -2.439   0.283  1.00  0.00           H  
HETATM   52  H19 UNL     1       4.383  -2.663  -0.889  1.00  0.00           H  
HETATM   53  H20 UNL     1       3.786  -0.398  -1.950  1.00  0.00           H  
HETATM   54  H21 UNL     1       1.491  -0.061  -1.996  1.00  0.00           H  
HETATM   55  H22 UNL     1       1.322  -2.025   0.460  1.00  0.00           H  
HETATM   56  H23 UNL     1       0.273  -2.064  -0.954  1.00  0.00           H  
HETATM   57  H24 UNL     1       0.771   0.370   0.964  1.00  0.00           H  
HETATM   58  H25 UNL     1      -1.536   0.786   0.798  1.00  0.00           H  
HETATM   59  H26 UNL     1      -2.538  -0.202  -1.260  1.00  0.00           H  
HETATM   60  H27 UNL     1      -1.529  -1.653  -1.234  1.00  0.00           H  
HETATM   61  H28 UNL     1      -2.505  -2.235   1.064  1.00  0.00           H  
HETATM   62  H29 UNL     1      -3.550  -0.777   0.918  1.00  0.00           H  
HETATM   63  H30 UNL     1      -3.275  -3.202  -0.942  1.00  0.00           H  
HETATM   64  H31 UNL     1      -4.672  -2.891   0.202  1.00  0.00           H  
HETATM   65  H32 UNL     1      -3.894  -1.236  -2.302  1.00  0.00           H  
HETATM   66  H33 UNL     1      -5.325  -2.353  -2.072  1.00  0.00           H  
HETATM   67  H34 UNL     1      -5.935   0.106  -1.707  1.00  0.00           H  
HETATM   68  H35 UNL     1      -4.768   0.148  -0.385  1.00  0.00           H  
HETATM   69  H36 UNL     1      -9.605  -2.242  -0.621  1.00  0.00           H  
HETATM   70  H37 UNL     1      -8.476  -3.042   0.568  1.00  0.00           H  
HETATM   71  H38 UNL     1     -10.235  -1.657   1.680  1.00  0.00           H  
HETATM   72  H39 UNL     1      -8.462  -1.561   3.000  1.00  0.00           H  
HETATM   73  H40 UNL     1     -10.461  -0.020  -0.179  1.00  0.00           H  
HETATM   74  H41 UNL     1      -8.803   0.617   0.255  1.00  0.00           H  
HETATM   75  H42 UNL     1     -12.210   2.446  -0.624  1.00  0.00           H  
HETATM   76  H43 UNL     1      -9.000   3.552   0.595  1.00  0.00           H  
CONECT    1    2   34   35   36
CONECT    2    3   37   38
CONECT    3    4   39   40
CONECT    4    5   41   42
CONECT    5    6   43   44
CONECT    6    7    7   45
CONECT    7    8   46
CONECT    8    9   47   48
CONECT    9   10   10   49
CONECT   10   11   50
CONECT   11   12   51   52
CONECT   12   13   13   53
CONECT   13   14   54
CONECT   14   15   55   56
CONECT   15   16   16   57
CONECT   16   17   58
CONECT   17   18   59   60
CONECT   18   19   61   62
CONECT   19   20   63   64
CONECT   20   21   65   66
CONECT   21   22   67   68
CONECT   22   23   23   24
CONECT   24   25
CONECT   25   26   69   70
CONECT   26   27   28   71
CONECT   27   72
CONECT   28   29   73   74
CONECT   29   30
CONECT   30   31   31   32   33
CONECT   32   75
CONECT   33   76
END

HMDB0062310
     RDKit          3D
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate
 76 75  0  0  0  0  0  0  0  0999 V2000
   11.9628    1.3544    1.0304 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0618    2.4876    0.6647 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8510    2.0356   -0.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0170    1.0504    0.6300 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8349    0.6646   -0.2747 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9981    1.7996   -0.6463 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7361    1.9828   -0.3759 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8228    1.1332    0.3582 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2345   -0.1023    0.9507 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8351   -1.2894    0.6854 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8702   -1.8005   -0.2695 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1788   -0.9369   -1.1907 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8936   -0.7555   -1.2334 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8794   -1.3953   -0.3461 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1805   -0.2943    0.3394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1009   -0.0757    0.2371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9761   -0.9176   -0.5825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0349   -1.5441    0.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9330   -2.4231   -0.4829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6184   -1.6259   -1.5557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4494   -0.5396   -0.9270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4703   -1.1672   -0.0512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1913   -1.4211    1.1371 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7128   -1.4692   -0.5346 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7829   -2.0429    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3137   -1.1895    1.2435 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.3968   -0.9336    2.2274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7343    0.1564    0.6410 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2841    0.8882    1.6932 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7914    2.4178    1.1334 P   0  0  0  0  0  5  0  0  0  0  0  0
  -10.9758    3.3687    2.2929 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2694    2.1553    0.3296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6852    3.0772    0.0556 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0041    1.5428    0.6359 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0059    1.2737    2.1513 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6673    0.3789    0.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6865    3.0652    1.5141 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6139    3.2022    0.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2360    1.6063   -1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2782    2.9439   -0.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6478    0.1561    0.8123 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6797    1.4120    1.5983 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4163    0.4137   -1.2556 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3901   -0.2831   -0.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4675    2.6300   -1.2401 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2790    2.9300   -0.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8771    1.0251   -0.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4176    1.8442    1.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0019    0.0039    1.7750 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3332   -2.0966    1.3204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1132   -2.4389    0.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3828   -2.6630   -0.8891 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7862   -0.3982   -1.9505 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4913   -0.0614   -1.9959 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3218   -2.0251    0.4604 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2735   -2.0638   -0.9540 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7714    0.3700    0.9641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5356    0.7864    0.7979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5380   -0.2021   -1.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5286   -1.6525   -1.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5054   -2.2346    1.0635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5502   -0.7774    0.9179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2754   -3.2021   -0.9416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6720   -2.8911    0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8938   -1.2362   -2.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3251   -2.3532   -2.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9353    0.1063   -1.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7678    0.1485   -0.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6046   -2.2422   -0.6210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4758   -3.0416    0.5677 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2352   -1.6567    1.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4616   -1.5611    2.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4606   -0.0199   -0.1789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8034    0.6166    0.2549 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2095    2.4456   -0.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0003    3.5516    0.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  2  0
 30 32  1  0
 30 33  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  0
  2 38  1  0
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  5 43  1  0
  5 44  1  0
  6 45  1  0
  7 46  1  0
  8 47  1  0
  8 48  1  0
  9 49  1  0
 10 50  1  0
 11 51  1  0
 11 52  1  0
 12 53  1  0
 13 54  1  0
 14 55  1  0
 14 56  1  0
 15 57  1  0
 16 58  1  0
 17 59  1  0
 17 60  1  0
 18 61  1  0
 18 62  1  0
 19 63  1  0
 19 64  1  0
 20 65  1  0
 20 66  1  0
 21 67  1  0
 21 68  1  0
 25 69  1  0
 25 70  1  0
 26 71  1  1
 27 72  1  0
 28 73  1  0
 28 74  1  0
 32 75  1  0
 33 76  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1-(7Z,10Z,13Z,16Z-Docosatetraenoyl)-glycero-3-phosphoric acid	Generator

Chemical Formula

C₂₅H₄₃O₇P

Average Molecular Weight

486.586

Monoisotopic Molecular Weight

486.274640723

IUPAC Name

[(2R)-3-[(7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoyloxy]-2-hydroxypropoxy]phosphonic acid

Traditional Name

(2R)-3-[(7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoyloxy]-2-hydroxypropoxyphosphonic acid

CAS Registry Number

Not Available

SMILES

[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCCCC(=O)OC[C@@]([H])(O)COP(O)(O)=O

InChI Identifier

InChI=1S/C25H43O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25(27)31-22-24(26)23-32-33(28,29)30/h6-7,9-10,12-13,15-16,24,26H,2-5,8,11,14,17-23H2,1H3,(H2,28,29,30)/b7-6-,10-9-,13-12-,16-15-/t24-/m1/s1

InChI Key

KSDVXYAHZXLGDS-XSQXPFHXSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-acylglycerol-3-phosphates. These are lysophosphatidic acids where the glycerol is esterified with a fatty acid at O-1 position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphates

Direct Parent

1-acylglycerol-3-phosphates

Alternative Parents

Substituents

1-acylglycerol-3-phosphate
Fatty acid ester
Monoalkyl phosphate
Fatty acyl
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Monoacylglycerophosphates (LMGP10050020 )

Ontology

Not Available

Exogenous (HMDB: HMDB0062310)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	0.0014 g/l	ALOGPS
LogP	5.67	ALOGPS

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	5.67	ALOGPS
logP	6.18	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	1.51	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	22	ChemAxon
Refractivity	137.05 m³·mol⁻¹	ChemAxon
Polarizability	55.31 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	227.899	31661259
DarkChem	[M-H]-	226.588	31661259
DeepCCS	[M+H]+	224.037	30932474
DeepCCS	[M-H]-	222.212	30932474
DeepCCS	[M-2H]-	255.452	30932474
DeepCCS	[M+Na]+	229.643	30932474
AllCCS	[M+H]+	222.7	32859911
AllCCS	[M+H-H2O]+	220.9	32859911
AllCCS	[M+NH4]+	224.3	32859911
AllCCS	[M+Na]+	224.8	32859911
AllCCS	[M-H]-	220.2	32859911
AllCCS	[M+Na-2H]-	224.0	32859911
AllCCS	[M+HCOO]-	228.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate	[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCCCC(=O)OC[C@@]([H])(O)COP(O)(O)=O	4484.3	Standard polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate	[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCCCC(=O)OC[C@@]([H])(O)COP(O)(O)=O	3059.8	Standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate	[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCCCC(=O)OC[C@@]([H])(O)COP(O)(O)=O	3680.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,1TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O)O)O[Si](C)(C)C	3685.9	Semi standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,1TMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@@H](O)COP(=O)(O)O[Si](C)(C)C	3648.0	Semi standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	3658.9	Semi standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	3347.4	Standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	4108.8	Standard polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3626.3	Semi standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3353.0	Standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3867.8	Standard polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,3TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3649.5	Semi standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,3TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3363.6	Standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,3TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3530.3	Standard polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,1TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O)O)O[Si](C)(C)C(C)(C)C	3920.2	Semi standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,1TBDMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@@H](O)COP(=O)(O)O[Si](C)(C)C(C)(C)C	3861.2	Semi standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4099.6	Semi standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3663.3	Standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4116.5	Standard polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TBDMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4066.6	Semi standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TBDMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3638.2	Standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,2TBDMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3951.8	Standard polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,3TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4285.2	Semi standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,3TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3750.4	Standard non polar	33892256
1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate,3TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3662.2	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate GC-MS (1 TMS) - 70eV, Positive	splash10-01p2-9241000000-7b5965b27f9cb6ef4b2d	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate 10V, Positive-QTOF	splash10-000i-0000900000-601aafd57da011fd1be4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate 20V, Positive-QTOF	splash10-000i-0000900000-601aafd57da011fd1be4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate 40V, Positive-QTOF	splash10-01b9-0905700000-6bafdd5f860494d6ad2c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate 10V, Negative-QTOF	splash10-000i-0000900000-292b722796d315e5d3dc	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate 20V, Negative-QTOF	splash10-000i-0000900000-292b722796d315e5d3dc	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate 40V, Negative-QTOF	splash10-0uei-2905600000-9fe63f94338559adab71	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

52929754

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Moritz A, De Graan PN, Gispen WH, Wirtz KW: Phosphatidic acid is a specific activator of phosphatidylinositol-4-phosphate kinase. J Biol Chem. 1992 Apr 15;267(11):7207-10. [PubMed:1313792 ]
Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
Divecha N, Irvine RF: Phospholipid signaling. Cell. 1995 Jan 27;80(2):269-78. [PubMed:7834746 ]
Moolenaar WH, Kruijer W, Tilly BC, Verlaan I, Bierman AJ, de Laat SW: Growth factor-like action of phosphatidic acid. Nature. 1986 Sep 11-17;323(6084):171-3. [PubMed:3748188 ]
Yang CY, Frohman MA: Mitochondria: signaling with phosphatidic acid. Int J Biochem Cell Biol. 2012 Aug;44(8):1346-50. doi: 10.1016/j.biocel.2012.05.006. Epub 2012 May 15. [PubMed:22609101 ]
Cevc, Gregor (1993). Phospholipids Handbook. Marcel Dekker.
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate (HMDB0062310)

MOL for HMDB0062310 (1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate)

3D MOL for HMDB0062310 (1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate)

3D SDF for HMDB0062310 (1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate)

3D-SDF for HMDB0062310 (1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate)

PDB for HMDB0062310 (1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate)

3D PDB for HMDB0062310 (1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate)

SMILES for HMDB0062310 (1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate)

INCHI for HMDB0062310 (1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate)

Structure for HMDB0062310 (1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate)

3D Structure for HMDB0062310 (1-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycero-3-phosphate)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra